Canonical Allele Identifier: PA338562
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys2553Gln
CA338557
NM_001127510.3:c.7657A>C